老年人 FTO 多态性与 COVID-19 死亡率之间的关系:一项基于人群的队列研究。

IF 4.6 2区 医学 Q1 INFECTIOUS DISEASES International Journal of Infectious Diseases Pub Date : 2024-11-01 Epub Date: 2024-09-06 DOI:10.1016/j.ijid.2024.107232
Jaroslav A. Hubacek , Nadezda Capkova , Martin Bobak , Hynek Pikhart
{"title":"老年人 FTO 多态性与 COVID-19 死亡率之间的关系:一项基于人群的队列研究。","authors":"Jaroslav A. Hubacek ,&nbsp;Nadezda Capkova ,&nbsp;Martin Bobak ,&nbsp;Hynek Pikhart","doi":"10.1016/j.ijid.2024.107232","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>COVID-19 caused a global pandemic with millions of deaths. Fat mass and obesity-associated gene (<em>FTO</em>) (alias m<sup>6</sup>A RNA demethylase) and its functional rs17817449 polymorphism are candidates to influence COVID-19-associated mortality since methylation status of viral nucleic acids is an important factor influencing viral viability.</div></div><div><h3>Methods</h3><div>We tested a population-based cohort of 5233 subjects (aged 63-87 years in 2020) where 70 persons died from COVID-19 and 394 from other causes during the pandemic period.</div></div><div><h3>Results</h3><div>The frequency of GG homozygotes was higher among those who died from COVID-19 (34%) than among survivors (19%) or deaths from other causes (20%), <em>P</em> &lt;0.005. After multiple adjustments, GG homozygotes had a higher risk of death from COVID-19 with odds ratio = 2.01 (95% confidence interval; 1.19-3.41, <em>P</em> &lt;0.01) compared with carriers of at least one T allele. The <em>FTO</em> polymorphism was not associated with mortality from other causes.</div></div><div><h3>Conclusions</h3><div>Our results suggest that <em>FTO</em> variability is a significant predictor of COVID-19-associated mortality in Caucasians.</div></div>","PeriodicalId":14006,"journal":{"name":"International Journal of Infectious Diseases","volume":"148 ","pages":"Article 107232"},"PeriodicalIF":4.6000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1201971224003035/pdfft?md5=4fa262b746807b7f5d8c637e0d19bd17&pid=1-s2.0-S1201971224003035-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Association between FTO polymorphism and COVID-19 mortality among older adults: A population-based cohort study\",\"authors\":\"Jaroslav A. Hubacek ,&nbsp;Nadezda Capkova ,&nbsp;Martin Bobak ,&nbsp;Hynek Pikhart\",\"doi\":\"10.1016/j.ijid.2024.107232\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objectives</h3><div>COVID-19 caused a global pandemic with millions of deaths. Fat mass and obesity-associated gene (<em>FTO</em>) (alias m<sup>6</sup>A RNA demethylase) and its functional rs17817449 polymorphism are candidates to influence COVID-19-associated mortality since methylation status of viral nucleic acids is an important factor influencing viral viability.</div></div><div><h3>Methods</h3><div>We tested a population-based cohort of 5233 subjects (aged 63-87 years in 2020) where 70 persons died from COVID-19 and 394 from other causes during the pandemic period.</div></div><div><h3>Results</h3><div>The frequency of GG homozygotes was higher among those who died from COVID-19 (34%) than among survivors (19%) or deaths from other causes (20%), <em>P</em> &lt;0.005. After multiple adjustments, GG homozygotes had a higher risk of death from COVID-19 with odds ratio = 2.01 (95% confidence interval; 1.19-3.41, <em>P</em> &lt;0.01) compared with carriers of at least one T allele. The <em>FTO</em> polymorphism was not associated with mortality from other causes.</div></div><div><h3>Conclusions</h3><div>Our results suggest that <em>FTO</em> variability is a significant predictor of COVID-19-associated mortality in Caucasians.</div></div>\",\"PeriodicalId\":14006,\"journal\":{\"name\":\"International Journal of Infectious Diseases\",\"volume\":\"148 \",\"pages\":\"Article 107232\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1201971224003035/pdfft?md5=4fa262b746807b7f5d8c637e0d19bd17&pid=1-s2.0-S1201971224003035-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Infectious Diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1201971224003035\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/9/6 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1201971224003035","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/9/6 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

摘要

目的:m6A RNA去甲基化酶(FTO)及其功能性rs17817449多态性可能会影响与COVID-19相关的死亡率,因为病毒核酸的甲基化状态是影响病毒生存能力的重要因素:我们对一个由 5180 名受试者(2020 年年龄为 63-87 岁)组成的人群队列进行了测试,在大流行期间,有 70 人死于 COVID-19,341 人死于其他原因:死于 COVID-19 的人群(34%)中的 GG 同源基因频率高于幸存者(19%)或死于其他原因的人群(20%),P < 0.005。经多重调整后,与至少一个T等位基因携带者相比,GG同源基因携带者死于COVID-19的风险更高,OR = 2.01 (95% CI; 1.19 - 3.41, p < 0.01)。FTO多态性与其他原因导致的死亡率无关:我们的研究结果表明,FTO变异是白种人COVID-19相关死亡率的重要预测因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Association between FTO polymorphism and COVID-19 mortality among older adults: A population-based cohort study

Objectives

COVID-19 caused a global pandemic with millions of deaths. Fat mass and obesity-associated gene (FTO) (alias m6A RNA demethylase) and its functional rs17817449 polymorphism are candidates to influence COVID-19-associated mortality since methylation status of viral nucleic acids is an important factor influencing viral viability.

Methods

We tested a population-based cohort of 5233 subjects (aged 63-87 years in 2020) where 70 persons died from COVID-19 and 394 from other causes during the pandemic period.

Results

The frequency of GG homozygotes was higher among those who died from COVID-19 (34%) than among survivors (19%) or deaths from other causes (20%), P <0.005. After multiple adjustments, GG homozygotes had a higher risk of death from COVID-19 with odds ratio = 2.01 (95% confidence interval; 1.19-3.41, P <0.01) compared with carriers of at least one T allele. The FTO polymorphism was not associated with mortality from other causes.

Conclusions

Our results suggest that FTO variability is a significant predictor of COVID-19-associated mortality in Caucasians.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
18.90
自引率
2.40%
发文量
1020
审稿时长
30 days
期刊介绍: International Journal of Infectious Diseases (IJID) Publisher: International Society for Infectious Diseases Publication Frequency: Monthly Type: Peer-reviewed, Open Access Scope: Publishes original clinical and laboratory-based research. Reports clinical trials, reviews, and some case reports. Focuses on epidemiology, clinical diagnosis, treatment, and control of infectious diseases. Emphasizes diseases common in under-resourced countries.
期刊最新文献
A systematic review and meta-analysis of bacterial pathogen prevalence in acute and chronic rhinosinusitis: implications for empiric antibiotic therapy and antimicrobial stewardship Real-world experience with cefiderocol in hematologic patients with malignancies Clinical and genomic characterization of pediatric adenovirus-associated severe acute respiratory infection: a binational study from Brazil and Colombia, 2022–2023 Comparative analysis of molecular protocols for detecting pfhrp2 and pfhrp3 gene deletions in Plasmodium falciparum samples from Rondônia, Brazilian Amazon Estimates of sexually transmitted infection prevalence and prevalence ratio among international migrants compared with non-migrants: A global systematic review and meta-analysis
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1